Hoeffel Guillaume, Ripoche Anne-Claire, Matheoud Diana, Nascimbeni Michelina, Escriou Nicolas, Lebon Pierre, Heshmati Farhad, Guillet Jean-Gérard, Gannagé Monique, Caillat-Zucman Sophie, Casartelli Nicoletta, Schwartz Olivier, De la Salle Henri, Hanau Daniel, Hosmalin Anne, Marañón Concepción
Département d'Immunologie, Institut Cochin, Paris, F-75014, France.
Immunity. 2007 Sep;27(3):481-92. doi: 10.1016/j.immuni.2007.07.021.
Crosspresentation is a specialized function of myeloid dendritic cells (mDCs), allowing them to induce CD8+ T cell responses against exogenous antigens that are not directly produced in their cytotosol. Human plasmacytoid DCs (pDCs) are not considered so far as able to perform crosspresentation. We showed here that purified human pDCs crosspresented vaccinal lipopeptides and HIV-1 antigens from apoptotic cells to specific CD8+ T lymphocytes. Apoptotic debris were internalized by phagocytosis and the lipopeptide LPPol reached nonacidic endosomes. This crosspresentation was amplified upon influenza virus infection. Importantly, the efficiency of crosspresentation by pDCs was comparable to that of mDCs. This property of human pDCs needs to be taken into account to understand the pathogenesis of infectious, allergic, or autimmune diseases and to help achieve desired responses during vaccination by targeting specifically either type of DCs.
交叉呈递是髓样树突状细胞(mDCs)的一种特殊功能,使它们能够诱导针对并非在其胞质溶胶中直接产生的外源性抗原的CD8 + T细胞反应。到目前为止,人类浆细胞样树突状细胞(pDCs)被认为不具备交叉呈递能力。我们在此表明,纯化的人类pDCs可将来自凋亡细胞的疫苗脂肽和HIV-1抗原交叉呈递给特异性CD8 + T淋巴细胞。凋亡碎片通过吞噬作用被内化,脂肽LPPol到达非酸性内体。这种交叉呈递在流感病毒感染后会增强。重要的是,pDCs的交叉呈递效率与mDCs相当。在理解感染性、过敏性或自身免疫性疾病的发病机制以及通过特异性靶向任何一种类型的树突状细胞来帮助在疫苗接种期间实现预期反应时,需要考虑人类pDCs的这一特性。